Active Ingredient
Pyrithione Zinc 0.5%
Wecare Anti-dandruff Liquid
FDA Label NDC 67777-139
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Dynarex Corporation for the product Wecare Anti-dandruff (NDC 67777-139). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient, purpose, use, warnings, when using this product, stop use and ask a doctor if, otc - keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Anti-Dandruff
Use
Helps eliminate irritation and flaking associated with dandruff
Warnings
For External Use Only
When Using This Product
- Avoid contact with eyes
- If contact occurs, rinse eyes with plenty of water
Stop Use And Ask A Doctor If
condition does not improve or worsens after regular use of this product as directed.
Otc - Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center immediately.
Directions
- wet hair
- lather
- massage onto scalp
- rinse well
- repeat if desired
- for best results, use regularly
Inactive Ingredients
Water, Sodium Laureth Sulfate, Cocamide MEA, Cocamidopropyl Betaine, Sodium Chloride, Glycol Distearate, Acrylates Copolymer, Coco-Glucoside, Styrene/Acrylates Copolymer, Dimethiconol, Glyceryl Oleate, Polyquaternium-10, Citric Acid, TEA-dodecyl-benzene-sulfonate, Sodium Hydroxide, Benzyl Alcohol, Sodium Benzoate, Methylchloroisothiazolinone, Methylisothiazolinone, Amyl Cinnamal, Benzyl Salicylate, CI42090
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